European Commission Updates MIR 7.3.1 Vigilance Reporting Forms
The European Commission has updated the MIR 7.3.1 vigilance reporting forms under the EU MDR and IVDR. Manufacturers should verify accepted versions and updated XSD/XSL files.
FDA Updates Coding Resources for Medical Device Reports: Key Changes from IMDRF 2025 Maintenance
FDA updates MDR adverse event codes under IMDRF 2025. Key changes may impact manufacturer reporting, vigilance systems, and data consistency.